DE3329070C2 - - Google Patents
Info
- Publication number
- DE3329070C2 DE3329070C2 DE3329070A DE3329070A DE3329070C2 DE 3329070 C2 DE3329070 C2 DE 3329070C2 DE 3329070 A DE3329070 A DE 3329070A DE 3329070 A DE3329070 A DE 3329070A DE 3329070 C2 DE3329070 C2 DE 3329070C2
- Authority
- DE
- Germany
- Prior art keywords
- image transfer
- sheet
- material according
- image
- radical
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000463 material Substances 0.000 claims description 69
- -1 alkyl radical Chemical group 0.000 claims description 48
- 239000000975 dye Substances 0.000 claims description 37
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 32
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 238000010521 absorption reaction Methods 0.000 claims description 16
- 125000005843 halogen group Chemical group 0.000 claims description 16
- 239000003086 colorant Substances 0.000 claims description 15
- 239000000945 filler Substances 0.000 claims description 14
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
- 125000003107 substituted aryl group Chemical group 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002825 nitriles Chemical class 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical group [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 4
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical class C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 claims description 3
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- JPIYZTWMUGTEHX-UHFFFAOYSA-N auramine O free base Chemical compound C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 JPIYZTWMUGTEHX-UHFFFAOYSA-N 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 2
- 239000000347 magnesium hydroxide Substances 0.000 claims description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 2
- 229950000688 phenothiazine Drugs 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 238000010186 staining Methods 0.000 claims description 2
- 239000011592 zinc chloride Substances 0.000 claims description 2
- 235000005074 zinc chloride Nutrition 0.000 claims description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims 1
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical class OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 claims 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 239000007788 liquid Substances 0.000 description 22
- 230000000052 comparative effect Effects 0.000 description 21
- 239000003921 oil Substances 0.000 description 15
- OQGRFQCUGLKSAV-JTQLQIEISA-N n-[(3s)-2,6-dioxopiperidin-3-yl]-2-phenylacetamide Chemical compound N([C@@H]1C(NC(=O)CC1)=O)C(=O)CC1=CC=CC=C1 OQGRFQCUGLKSAV-JTQLQIEISA-N 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 12
- 238000007651 thermal printing Methods 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 8
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 8
- 239000001856 Ethyl cellulose Substances 0.000 description 7
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 7
- 229920001249 ethyl cellulose Polymers 0.000 description 7
- 235000019325 ethyl cellulose Nutrition 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 6
- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 6
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 6
- FJKROLUGYXJWQN-UHFFFAOYSA-M 4-hydroxybenzoate Chemical compound OC1=CC=C(C([O-])=O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-M 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 150000002989 phenols Chemical class 0.000 description 5
- 229920006267 polyester film Polymers 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 239000005711 Benzoic acid Substances 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 235000010233 benzoic acid Nutrition 0.000 description 4
- HWEOYOXBRATLKT-UHFFFAOYSA-N n-octadecylbenzamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C1=CC=CC=C1 HWEOYOXBRATLKT-UHFFFAOYSA-N 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229960004889 salicylic acid Drugs 0.000 description 4
- APMWEQQELZTXTL-UHFFFAOYSA-N (2-methoxyphenyl) 2-hydroxybenzoate Chemical compound COC1=CC=CC=C1OC(=O)C1=CC=CC=C1O APMWEQQELZTXTL-UHFFFAOYSA-N 0.000 description 3
- 206010057040 Temperature intolerance Diseases 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical group C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 3
- 239000004203 carnauba wax Substances 0.000 description 3
- 235000013869 carnauba wax Nutrition 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000008543 heat sensitivity Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- GJLNWLVPAHNBQN-UHFFFAOYSA-N phenyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1 GJLNWLVPAHNBQN-UHFFFAOYSA-N 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 229920006255 plastic film Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- SULYEHHGGXARJS-UHFFFAOYSA-N 2',4'-dihydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1O SULYEHHGGXARJS-UHFFFAOYSA-N 0.000 description 2
- NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- IMHDGJOMLMDPJN-UHFFFAOYSA-N biphenyl-2,2'-diol Chemical group OC1=CC=CC=C1C1=CC=CC=C1O IMHDGJOMLMDPJN-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- OOCSVLHOTKHEFZ-UHFFFAOYSA-N icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(N)=O OOCSVLHOTKHEFZ-UHFFFAOYSA-N 0.000 description 2
- GPSDUZXPYCFOSQ-UHFFFAOYSA-N m-toluic acid Chemical compound CC1=CC=CC(C(O)=O)=C1 GPSDUZXPYCFOSQ-UHFFFAOYSA-N 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- OSLMDZTZEPAYCP-UHFFFAOYSA-N n-cyclohexylpropanamide Chemical compound CCC(=O)NC1CCCCC1 OSLMDZTZEPAYCP-UHFFFAOYSA-N 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- CHIJIQHKEIBUPB-UHFFFAOYSA-N (2,3-dichlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC(Cl)=C1Cl CHIJIQHKEIBUPB-UHFFFAOYSA-N 0.000 description 1
- RHEZJKZNYHZXMR-UHFFFAOYSA-N (2,4,6-trichlorophenyl) benzoate Chemical compound ClC1=CC(Cl)=CC(Cl)=C1OC(=O)C1=CC=CC=C1 RHEZJKZNYHZXMR-UHFFFAOYSA-N 0.000 description 1
- YMWXQUBFDGEVNI-UHFFFAOYSA-N (2,4-dibromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Br)C=C1Br YMWXQUBFDGEVNI-UHFFFAOYSA-N 0.000 description 1
- WHWSHWZIJIZSIG-UHFFFAOYSA-N (2,4-dibromophenyl) benzoate Chemical compound BrC1=CC(Br)=CC=C1OC(=O)C1=CC=CC=C1 WHWSHWZIJIZSIG-UHFFFAOYSA-N 0.000 description 1
- UNNUESFABWIRHI-UHFFFAOYSA-N (2,4-dichlorophenyl) benzoate Chemical compound ClC1=CC(Cl)=CC=C1OC(=O)C1=CC=CC=C1 UNNUESFABWIRHI-UHFFFAOYSA-N 0.000 description 1
- YBFZUTPPMWWFLT-UHFFFAOYSA-N (2,4-dimethylphenyl) 2-hydroxybenzoate Chemical compound CC1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1O YBFZUTPPMWWFLT-UHFFFAOYSA-N 0.000 description 1
- RRTHUXNSBDKADU-UHFFFAOYSA-N (2,6-dichloro-4-methylphenyl) benzoate Chemical compound ClC1=CC(C)=CC(Cl)=C1OC(=O)C1=CC=CC=C1 RRTHUXNSBDKADU-UHFFFAOYSA-N 0.000 description 1
- VPGDZNFUPPCJOB-UHFFFAOYSA-N (2-acetyloxyphenyl) benzoate Chemical compound CC(=O)OC1=CC=CC=C1OC(=O)C1=CC=CC=C1 VPGDZNFUPPCJOB-UHFFFAOYSA-N 0.000 description 1
- CBLBPSNUGAXWGH-UHFFFAOYSA-N (2-benzoyl-5-methylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC(C)=CC=C1C(=O)C1=CC=CC=C1 CBLBPSNUGAXWGH-UHFFFAOYSA-N 0.000 description 1
- LVTPRIAGCBEGPW-UHFFFAOYSA-N (2-benzoyloxyphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1OC(=O)C1=CC=CC=C1 LVTPRIAGCBEGPW-UHFFFAOYSA-N 0.000 description 1
- FWSWFCIRSUDUOM-UHFFFAOYSA-N (2-chlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1Cl FWSWFCIRSUDUOM-UHFFFAOYSA-N 0.000 description 1
- WIRVGPKLACEVRA-UHFFFAOYSA-N (2-ethoxyphenyl) 2-hydroxybenzoate Chemical class CCOC1=CC=CC=C1OC(=O)C1=CC=CC=C1O WIRVGPKLACEVRA-UHFFFAOYSA-N 0.000 description 1
- RFIRCRFSWDHEBP-UHFFFAOYSA-N (2-methoxy-4-methylphenyl) 4-hydroxybenzoate Chemical compound COC1=CC(C)=CC=C1OC(=O)C1=CC=C(O)C=C1 RFIRCRFSWDHEBP-UHFFFAOYSA-N 0.000 description 1
- YHCOQZVGVFISLR-UHFFFAOYSA-N (2-methoxyphenyl) 4-hydroxybenzoate Chemical compound COC1=CC=CC=C1OC(=O)C1=CC=C(O)C=C1 YHCOQZVGVFISLR-UHFFFAOYSA-N 0.000 description 1
- ALYKUDRBSKNACP-UHFFFAOYSA-N (3-bromophenyl) benzoate Chemical compound BrC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 ALYKUDRBSKNACP-UHFFFAOYSA-N 0.000 description 1
- TVFLZSCYOACNAS-UHFFFAOYSA-N (3-hydroxyphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 TVFLZSCYOACNAS-UHFFFAOYSA-N 0.000 description 1
- BCUFQMVZYDFSIG-UHFFFAOYSA-N (3-iodophenyl) benzoate Chemical compound IC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 BCUFQMVZYDFSIG-UHFFFAOYSA-N 0.000 description 1
- QKOXLEURWZTLAY-UHFFFAOYSA-N (3-methoxyphenyl) 2-hydroxybenzoate Chemical compound COC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 QKOXLEURWZTLAY-UHFFFAOYSA-N 0.000 description 1
- WYCMXEZEGOOMSO-UHFFFAOYSA-N (3-methylphenyl) 2-hydroxybenzoate Chemical compound CC1=CC=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 WYCMXEZEGOOMSO-UHFFFAOYSA-N 0.000 description 1
- JWLQSDXEKWFFBU-UHFFFAOYSA-N (3-nitrophenyl) benzoate Chemical compound [O-][N+](=O)C1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 JWLQSDXEKWFFBU-UHFFFAOYSA-N 0.000 description 1
- DLLWMHSSGQYZPE-UHFFFAOYSA-N (4-benzoylphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C(=O)C=2C=CC=CC=2)C=C1 DLLWMHSSGQYZPE-UHFFFAOYSA-N 0.000 description 1
- MCDYTRXHCNELKZ-UHFFFAOYSA-N (4-benzoylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=C1)=CC=C1C(=O)C1=CC=CC=C1 MCDYTRXHCNELKZ-UHFFFAOYSA-N 0.000 description 1
- XSGIPGFJYOYADV-UHFFFAOYSA-N (4-benzylphenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC(C=C1)=CC=C1CC1=CC=CC=C1 XSGIPGFJYOYADV-UHFFFAOYSA-N 0.000 description 1
- QMMQPXSGXXDYHG-UHFFFAOYSA-N (4-benzylphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=C1)=CC=C1CC1=CC=CC=C1 QMMQPXSGXXDYHG-UHFFFAOYSA-N 0.000 description 1
- INUXCUFFKPBMKK-UHFFFAOYSA-N (4-bromophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Br)C=C1 INUXCUFFKPBMKK-UHFFFAOYSA-N 0.000 description 1
- NMPRZRJMGXDQJH-UHFFFAOYSA-N (4-butoxyphenyl) 4-hydroxybenzoate Chemical compound C1=CC(OCCCC)=CC=C1OC(=O)C1=CC=C(O)C=C1 NMPRZRJMGXDQJH-UHFFFAOYSA-N 0.000 description 1
- SUEYSYGFYRKFKO-UHFFFAOYSA-N (4-chloro-2-methylphenyl) benzoate Chemical compound CC1=CC(Cl)=CC=C1OC(=O)C1=CC=CC=C1 SUEYSYGFYRKFKO-UHFFFAOYSA-N 0.000 description 1
- CDBOTLBWQJJKQJ-UHFFFAOYSA-N (4-chloro-3-methylphenyl) 2-hydroxybenzoate Chemical compound C1=C(Cl)C(C)=CC(OC(=O)C=2C(=CC=CC=2)O)=C1 CDBOTLBWQJJKQJ-UHFFFAOYSA-N 0.000 description 1
- TUYYMOBSJNEIKN-UHFFFAOYSA-N (4-chlorophenyl) 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(Cl)C=C1 TUYYMOBSJNEIKN-UHFFFAOYSA-N 0.000 description 1
- BXXPTNJQVHYLIK-UHFFFAOYSA-N (4-chlorophenyl) 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=C(Cl)C=C1 BXXPTNJQVHYLIK-UHFFFAOYSA-N 0.000 description 1
- CHMPIVCGVXDTTL-UHFFFAOYSA-N (4-ethoxycarbonylphenyl) 4-methoxybenzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1OC(=O)C1=CC=C(OC)C=C1 CHMPIVCGVXDTTL-UHFFFAOYSA-N 0.000 description 1
- HXUSROHSMQXTIY-UHFFFAOYSA-N (4-ethoxycarbonylphenyl) 4-methylbenzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1OC(=O)C1=CC=C(C)C=C1 HXUSROHSMQXTIY-UHFFFAOYSA-N 0.000 description 1
- UFNKAYBBJKLRIW-UHFFFAOYSA-N (4-hydroxyphenyl) 2-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1OC(=O)C1=CC=CC=C1O UFNKAYBBJKLRIW-UHFFFAOYSA-N 0.000 description 1
- KVFFCZXWUPJFFQ-UHFFFAOYSA-N (4-methoxyphenyl) 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1OC(=O)C1=CC=C(OC)C=C1 KVFFCZXWUPJFFQ-UHFFFAOYSA-N 0.000 description 1
- PMRMHHUTWZPFIY-UHFFFAOYSA-N (4-methoxyphenyl) benzoate Chemical compound C1=CC(OC)=CC=C1OC(=O)C1=CC=CC=C1 PMRMHHUTWZPFIY-UHFFFAOYSA-N 0.000 description 1
- MJLXQKNXJKYSOA-UHFFFAOYSA-N (4-methylphenyl) 2-nitrobenzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1[N+]([O-])=O MJLXQKNXJKYSOA-UHFFFAOYSA-N 0.000 description 1
- VXCLPVZGTDMDND-UHFFFAOYSA-N (4-methylphenyl) 4-nitrobenzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=C([N+]([O-])=O)C=C1 VXCLPVZGTDMDND-UHFFFAOYSA-N 0.000 description 1
- LLRZUDIHEZXFGV-UHFFFAOYSA-N (4-methylphenyl) benzoate Chemical compound C1=CC(C)=CC=C1OC(=O)C1=CC=CC=C1 LLRZUDIHEZXFGV-UHFFFAOYSA-N 0.000 description 1
- GFLGTOLWFQLOPT-UHFFFAOYSA-N (4-naphthalen-1-ylphenyl) benzoate Chemical compound C=1C=C(C=2C3=CC=CC=C3C=CC=2)C=CC=1OC(=O)C1=CC=CC=C1 GFLGTOLWFQLOPT-UHFFFAOYSA-N 0.000 description 1
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- JJOVCQBPDCSFDT-UHFFFAOYSA-N n-methylnonadecanamide Chemical compound CCCCCCCCCCCCCCCCCCC(=O)NC JJOVCQBPDCSFDT-UHFFFAOYSA-N 0.000 description 1
- PMNNKCGDKSIBLA-UHFFFAOYSA-N n-octadecyl-2-phenylacetamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CC1=CC=CC=C1 PMNNKCGDKSIBLA-UHFFFAOYSA-N 0.000 description 1
- UOJWCKBTLPPNFI-UHFFFAOYSA-N n-octadecylcyclohexanecarboxamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)C1CCCCC1 UOJWCKBTLPPNFI-UHFFFAOYSA-N 0.000 description 1
- FLWVQJFJIXHMAY-UHFFFAOYSA-N n-propyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCC FLWVQJFJIXHMAY-UHFFFAOYSA-N 0.000 description 1
- GHLZUHZBBNDWHW-UHFFFAOYSA-N nonanamide Chemical compound CCCCCCCCC(N)=O GHLZUHZBBNDWHW-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 description 1
- KLAKIAVEMQMVBT-UHFFFAOYSA-N p-hydroxy-phenacyl alcohol Natural products OCC(=O)C1=CC=C(O)C=C1 KLAKIAVEMQMVBT-UHFFFAOYSA-N 0.000 description 1
- RQGCQWARLQDMCZ-UHFFFAOYSA-N pentadecanamide Chemical compound CCCCCCCCCCCCCCC(N)=O RQGCQWARLQDMCZ-UHFFFAOYSA-N 0.000 description 1
- LIDDQKAMUXHIQD-UHFFFAOYSA-N phenyl 2-benzoyloxybenzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 LIDDQKAMUXHIQD-UHFFFAOYSA-N 0.000 description 1
- CZEPEQHOBBKCSQ-UHFFFAOYSA-N phenyl 4-acetyloxybenzoate Chemical compound C1=CC(OC(=O)C)=CC=C1C(=O)OC1=CC=CC=C1 CZEPEQHOBBKCSQ-UHFFFAOYSA-N 0.000 description 1
- BNZYBNYNPXKWCM-UHFFFAOYSA-N phenyl 4-methoxybenzoate Chemical compound C1=CC(OC)=CC=C1C(=O)OC1=CC=CC=C1 BNZYBNYNPXKWCM-UHFFFAOYSA-N 0.000 description 1
- WOHDXQQIBRMRFA-UHFFFAOYSA-N phenyl 4-methylbenzoate Chemical compound C1=CC(C)=CC=C1C(=O)OC1=CC=CC=C1 WOHDXQQIBRMRFA-UHFFFAOYSA-N 0.000 description 1
- NVGUCNZOTBWESS-UHFFFAOYSA-N phenyl 4-phenoxybenzoate Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1C(=O)OC1=CC=CC=C1 NVGUCNZOTBWESS-UHFFFAOYSA-N 0.000 description 1
- PSBAIJVSCTZDDB-UHFFFAOYSA-N phenyl acetylsalicylate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 PSBAIJVSCTZDDB-UHFFFAOYSA-N 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- ZAYKUYSGARCXKQ-UHFFFAOYSA-N tetracosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(N)=O ZAYKUYSGARCXKQ-UHFFFAOYSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/38235—Contact thermal transfer or sublimation processes characterised by transferable colour-forming materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/40—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used characterised by the base backcoat, intermediate, or covering layers, e.g. for thermal transfer dye-donor or dye-receiver sheets; Heat, radiation filtering or absorbing means or layers; combined with other image registration layers or compositions; Special originals for reproduction by thermography
- B41M5/41—Base layers supports or substrates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5218—Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5227—Macromolecular coatings characterised by organic non-macromolecular additives, e.g. UV-absorbers, plasticisers, surfactants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Color Printing (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57139347A JPS5929193A (ja) | 1982-08-11 | 1982-08-11 | 感熱転写媒体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE3329070A1 DE3329070A1 (de) | 1984-03-01 |
| DE3329070C2 true DE3329070C2 (enrdf_load_stackoverflow) | 1989-03-23 |
Family
ID=15243207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19833329070 Granted DE3329070A1 (de) | 1982-08-11 | 1983-08-11 | Waermeempfindliches bilduebertragungsmaterial |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US4547788A (enrdf_load_stackoverflow) |
| JP (1) | JPS5929193A (enrdf_load_stackoverflow) |
| DE (1) | DE3329070A1 (enrdf_load_stackoverflow) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4575734A (en) * | 1982-08-19 | 1986-03-11 | Ricoh Company, Ltd. | Thermosensitive image transfer medium |
| JPH0739207B2 (ja) * | 1984-04-17 | 1995-05-01 | 住友化学工業株式会社 | 転写型感熱記録方法 |
| JPS60222282A (ja) * | 1984-04-19 | 1985-11-06 | Ricoh Co Ltd | 多色画像記録方法 |
| EP0199368B1 (en) * | 1985-04-26 | 1991-02-06 | Sony Corporation | Printing paper for thermal transfer printing |
| JPS61274988A (ja) * | 1985-05-31 | 1986-12-05 | Toppan Moore Co Ltd | 感熱複写シ−ト |
| AU593591B2 (en) * | 1985-11-08 | 1990-02-15 | Fuji Photo Film Co., Ltd. | Recording material |
| US4879268A (en) * | 1987-03-30 | 1989-11-07 | Sheldon Dunstan P | Multiple document parallel printing apparatus |
| US5318943A (en) * | 1991-05-27 | 1994-06-07 | Dai Nippon Printing Co., Ltd. | Thermal transfer image receiving sheet |
| JP4814011B2 (ja) * | 2006-08-15 | 2011-11-09 | 日清フーズ株式会社 | ピザ生地の成形装置及びこの成形装置を使用したピザ生地の成形方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5386229A (en) * | 1977-01-07 | 1978-07-29 | Kanzaki Paper Mfg Co Ltd | Thermosensitive recording body |
| JPS53118059A (en) * | 1977-03-25 | 1978-10-16 | Mitsubishi Paper Mills Ltd | Thermosensitive paper in which adhesiveness of refuses to thermal head be improved |
| JPS5423545A (en) * | 1977-07-22 | 1979-02-22 | Mitsubishi Paper Mills Ltd | Heat sensitive paper with reduced adherability of dregs to thermal head |
| JPS5553592A (en) * | 1978-10-16 | 1980-04-19 | Fuji Photo Film Co Ltd | Recording material |
| JPS5834313B2 (ja) * | 1980-05-13 | 1983-07-26 | 株式会社リコー | 感熱記録材料 |
| US4355070A (en) * | 1980-12-01 | 1982-10-19 | Kanzaki Paper Manufacturing Co., Ltd. | Heat-sensitive record material |
-
1982
- 1982-08-11 JP JP57139347A patent/JPS5929193A/ja active Granted
-
1983
- 1983-07-21 US US06/516,180 patent/US4547788A/en not_active Expired - Fee Related
- 1983-08-11 DE DE19833329070 patent/DE3329070A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| US4547788A (en) | 1985-10-15 |
| JPH0157679B2 (enrdf_load_stackoverflow) | 1989-12-06 |
| DE3329070A1 (de) | 1984-03-01 |
| JPS5929193A (ja) | 1984-02-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OP8 | Request for examination as to paragraph 44 patent law | ||
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |